Nitrogen-centred helical acridiniums with a 6–7–6–6 fused ring skeleton
Abstract
oxidative ring contraction of a helical azaheptalene. X-ray, spectroscopic, and theoretical studies revealed highly distorted, configurationally stable helicity with long-wavelength absorption and chiroptical properties. These findings provide a new π-conjugated helical framework for functional chiral materials.
Fields of Study & Subjects
Synthesis and Properties of Aromatic Compounds
Axial and Atropisomeric Chirality Synthesis
Photochromic and Fluorescence Chemistry
Publication details
- Journal / source
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 62
- Issue
- 14
- Pages
- 4268–4271
- Publication date
- 1 January 2026
- Language
- EN